APA

Mefford H. C., Shafer N., Antonacci F., Tsai J. M., Park S. S., Hing A. V., Rieder M. J., Smyth M. D., Speltz M. L., Eichler E. E. & Cunningham M. L. (20101215). Copy number variation analysis in single-suture craniosynostosis: multiple rare variants including RUNX2 duplication in two cousins with metopic craniosynostosis. : American journal of medical genetics. Part A.

Chicago

Mefford Heather C, Shafer Neil, Antonacci Francesca, Tsai Jesse M, Park Sarah S, Hing Anne V, Rieder Mark J, Smyth Matthew D, Speltz Matthew L, Eichler Evan E and Cunningham Michael L. 20101215. Copy number variation analysis in single-suture craniosynostosis: multiple rare variants including RUNX2 duplication in two cousins with metopic craniosynostosis. : American journal of medical genetics. Part A.

Harvard

Mefford H. C., Shafer N., Antonacci F., Tsai J. M., Park S. S., Hing A. V., Rieder M. J., Smyth M. D., Speltz M. L., Eichler E. E. and Cunningham M. L. (20101215). Copy number variation analysis in single-suture craniosynostosis: multiple rare variants including RUNX2 duplication in two cousins with metopic craniosynostosis. : American journal of medical genetics. Part A.

MLA

Mefford Heather C, Shafer Neil, Antonacci Francesca, Tsai Jesse M, Park Sarah S, Hing Anne V, Rieder Mark J, Smyth Matthew D, Speltz Matthew L, Eichler Evan E and Cunningham Michael L. Copy number variation analysis in single-suture craniosynostosis: multiple rare variants including RUNX2 duplication in two cousins with metopic craniosynostosis. : American journal of medical genetics. Part A. 20101215.